A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275413



Internal ID348319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87026620..87027287hg38UCSC Ensembl
Outerchr9:87023216..87028894hg38UCSC Ensembl
Innerchr9:89641535..89642202hg19UCSC Ensembl
Outerchr9:89638131..89643809hg19UCSC Ensembl
Innerchr9:88831355..88832022hg18UCSC Ensembl
Outerchr9:88827951..88833629hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg385679
hg195679
hg185679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585898
Samples
Known GenesLOC440173
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275413
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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